Device recall
Z-1023-04: Model 511 Cardio Respiratory Monitor with Oximax technology with software…
FDA device recall · Class II · CAS Medical Systems, Inc.
Key facts
| Recall number (Z-number) | Z-1023-04 |
|---|---|
| Recall event | 29223 |
| Product | Model 511 Cardio Respiratory Monitor with Oximax technology with software version 5.0 |
| Product code | BZQ |
| Recalling firm | CAS Medical Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 13, 2005 |
| 510(k) numbers | K962781 |
| FEI number | 2244861 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database